JP2018530582A5 - - Google Patents

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Publication number
JP2018530582A5
JP2018530582A5 JP2018519276A JP2018519276A JP2018530582A5 JP 2018530582 A5 JP2018530582 A5 JP 2018530582A5 JP 2018519276 A JP2018519276 A JP 2018519276A JP 2018519276 A JP2018519276 A JP 2018519276A JP 2018530582 A5 JP2018530582 A5 JP 2018530582A5
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JP
Japan
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substituted
halo
alkyl
compound according
phenyl
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JP2018519276A
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English (en)
Japanese (ja)
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JP2018530582A (ja
JP6843853B2 (ja
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Priority claimed from PCT/US2016/056716 external-priority patent/WO2017066368A1/en
Publication of JP2018530582A publication Critical patent/JP2018530582A/ja
Publication of JP2018530582A5 publication Critical patent/JP2018530582A5/ja
Application granted granted Critical
Publication of JP6843853B2 publication Critical patent/JP6843853B2/ja
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JP2018519276A 2015-10-14 2016-10-13 選択的nr2bアンタゴニスト Active JP6843853B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
IN3309DE2015 2015-10-14
IN3309/DEL/2015 2015-10-14
PCT/US2016/056716 WO2017066368A1 (en) 2015-10-14 2016-10-13 Selective nr2b antagonists

Publications (3)

Publication Number Publication Date
JP2018530582A JP2018530582A (ja) 2018-10-18
JP2018530582A5 true JP2018530582A5 (hr) 2019-11-21
JP6843853B2 JP6843853B2 (ja) 2021-03-17

Family

ID=57208377

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2018519276A Active JP6843853B2 (ja) 2015-10-14 2016-10-13 選択的nr2bアンタゴニスト

Country Status (13)

Country Link
US (2) US10501451B2 (hr)
EP (1) EP3362447B1 (hr)
JP (1) JP6843853B2 (hr)
KR (1) KR20180064507A (hr)
CN (1) CN108368101B (hr)
AU (1) AU2016340239A1 (hr)
BR (1) BR112018007181A2 (hr)
CA (1) CA3001894A1 (hr)
EA (1) EA201890764A1 (hr)
ES (1) ES2822830T3 (hr)
IL (1) IL258611A (hr)
MX (1) MX2018004257A (hr)
WO (1) WO2017066368A1 (hr)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2818254T3 (es) * 2015-10-14 2021-04-09 Bristol Myers Squibb Co Antagonistas selectivos de NR2B
BR112021004993A2 (pt) * 2018-10-17 2021-06-08 Boehringer Ingelheim International Gmbh derivados de 4-pirqazin-2-ilmetil-morfolina e o uso dos mesmos com medicamento
JP7093470B2 (ja) * 2018-10-17 2022-06-29 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング 4-ピリミジン-5-イルメチル-モルホリン誘導体および医薬としてのその使用
CN112867508B (zh) * 2018-10-17 2023-09-15 勃林格殷格翰国际有限公司 4-吡啶基甲基-吗啉衍生物及其作为药物的用途
TW202237103A (zh) * 2020-12-04 2022-10-01 瑞士商諾華公司 用於治療抑鬱症的nr2b-nmda受體nam之劑量方案
CN113620896A (zh) * 2021-08-31 2021-11-09 青岛科技大学 2-(2-氯苯基)甲基-4,4-二甲基-3-异恶唑酮的制备方法

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6476041B1 (en) 1999-10-29 2002-11-05 Merck & Co., Inc. 1,4 substituted piperidinyl NMDA/NR2B antagonists
US7022728B2 (en) 2001-03-09 2006-04-04 Abbott Laboratories Benzimidazoles that are useful in treating male sexual dysfunction
WO2003035641A1 (fr) 2001-10-22 2003-05-01 Shionogi & Co., Ltd. Nouveau derive carbamoyl-pyrrolidone
ATE403651T1 (de) 2003-06-04 2008-08-15 Merck & Co Inc 3-fluoro-piperidine als nmda/nr2b antagonisten
EP1673367A1 (en) 2003-10-08 2006-06-28 Pfizer, Inc. Fused lactam compounds
EP1736474A4 (en) * 2004-04-07 2010-04-21 Kyowa Hakko Kirin Co Ltd piperidine
JPWO2006137465A1 (ja) * 2005-06-24 2009-01-22 塩野義製薬株式会社 含窒素複素環誘導体
US7935706B2 (en) 2006-02-23 2011-05-03 Shionogi & Co., Ltd. Nitrogen-containing heterocycle derivatives substituted with cyclic group
CN103497114A (zh) 2007-06-29 2014-01-08 埃莫里大学 用于神经保护的nmda受体拮抗剂
JP2009067784A (ja) * 2007-08-21 2009-04-02 Shionogi & Co Ltd 環式基で置換された含窒素複素環誘導体を含有する鎮痛剤
SG10201811584RA (en) * 2010-02-11 2019-01-30 Univ Northwestern Secondary Structure Stabilized NMDA Receptor Modulators And Uses Thereof
US9187506B2 (en) * 2014-01-09 2015-11-17 Bristol-Myers Squibb Company (R)-3-((3S,4S)-3-fluoro-4-(4-hydroxyphenyl)piperidin-1-yl)-1-(4-methylbenzyl)pyrrolidin-2-one and its prodrugs for the treatment of psychiatric disorders
US9221796B2 (en) 2014-01-09 2015-12-29 Bristol-Myers Squibb Company Selective NR2B antagonists

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